ICAM5

Intercellular adhesion molecule 5 Q9UMF0 ICAM5_HUMAN
Protein Coding Chr 19 19p13.2 Swiss-Prot reviewed Entrez 7087
Mutations
491
CL 111 · Tissue 367
Samples
434
CL 89 · Tissue 335
Peptides
337
unique mutant peptides
Transcripts
1
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations491111367
Samples43489335
Peptides33769277

Function

ICAM5 · Intercellular adhesion molecule 5

The protein encoded by this gene is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins, contain 2-9 immunoglobulin-like C2-type domains, and bind to the leukocyte adhesion LFA-1 protein. This protein is expressed on the surface of telencephalic neurons and displays two types of adhesion activity, homophilic binding between neurons and heterophilic binding between neurons and leukocytes. It may be a critical component in neuron-microglial cell interactions in the course of normal development or as part of neurodegenerative diseases. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000221980 Q9UMF0 491 337

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.2
Entrez ID
Aliases
TLCNTLN

Recurrent Mutations

All 337 amino-acid changes on canonical ENST00000221980 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in ICAM5 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in ICAM5 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
13/40 32%
0/0 0%
Glioblastoma
3/98 3%
0/0 0%
Endometrial Carcinoma
4/42 10%
13/612 2%
Colorectal Carcinoma
17/143 12%
56/3239 2%
Gastric Carcinoma
3/74 4%
37/1809 2%
Bladder Carcinoma
2/58 3%
18/956 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Other Solid Cancers
2/94 2%
25/1515 2%
Melanoma
2/210 1%
31/1899 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Cervical Carcinoma
0/35 0%
6/422 1%
Biliary Tract Carcinoma
2/54 4%
11/950 1%
Plasma Cell Myeloma
2/44 5%
2/305 1%
Esophageal Carcinoma
2/23 9%
7/769 1%
Non-Small Cell Lung Carcinoma
2/304 1%
16/1390 1%
Ovarian Carcinoma
5/109 5%
6/998 1%
Squamous Cell Lung Carcinoma
0/57 0%
8/810 1%
Hepatocellular Carcinoma
2/46 4%
16/2210 1%
Other Sarcomas
0/69 0%
6/699 1%
Head and Neck Carcinoma
0/85 0%
13/1574 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
18/2550 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Osteosarcoma
0/45 0%
1/166 1%
Mesothelioma
1/62 2%
0/165 0%
Glioma
1/52 2%
8/2127 0%
Meningioma
1/3 33%
0/252 0%
Breast Carcinoma
5/144 3%
8/3264 0%

Mutation Distribution

Where ICAM5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ICAM5 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 491 mutations in ICAM5

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide